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2814-60-0

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2814-60-0 Usage

General Description

The chemical "(2Z)-3-ethyl-2-[(2E)-(3-ethyl-1,3-benzothiazol-2(3H)-ylidene)hydrazono]-2,3-dihydro-1,3-benzothiazole" is a complex organic compound with a molecular formula C17H19N3S2. It contains both a benzothiazole ring and an ethyl group, and has a hydrazono group attached to the benzothiazole ring. This chemical has potential applications in various fields including pharmaceuticals, agriculture, and materials science. However, due to its complex structure and potentially reactive hydrazono group, this compound requires careful handling and further research to fully understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 2814-60-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,1 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2814-60:
(6*2)+(5*8)+(4*1)+(3*4)+(2*6)+(1*0)=80
80 % 10 = 0
So 2814-60-0 is a valid CAS Registry Number.

2814-60-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-ethyl-N-[(Z)-(3-ethyl-1,3-benzothiazol-2-ylidene)amino]-1,3-benzothiazol-2-imine

1.2 Other means of identification

Product number -
Other names Bis-<3-aethyl-benzthiazolinyliden>-hydrazin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2814-60-0 SDS

2814-60-0Downstream Products

2814-60-0Relevant articles and documents

Excited state electronic structures and photochemistry of different oxidation states of 2,2′-azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS)

Ji, Feixiang,Guo, Yurong,Wang, Mengqi,Wu, Zibo,Shi, Yanan,Zhao, Xiaoying,Wang, Haiyuan,Feng, Xia,Zhao, Guangjiu

, (2021)

The molecular structures of 2,2-azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS), were calculated by using time-dependent density functional theory (TDDFT) model with M062X method with 6-311G (d, p) basis set. In this work, the ABTS were theoreti

Preparation method of 2, 2'-azino-bis(3-alkylbenzothiazoline-6-sulfonic acid) salt

-

, (2020/11/23)

The invention discloses a preparation method of a 2, 2'-azino-bis(3-alkylbenzothiazoline-6-sulfonic acid) salt. The raw materials used in the preparation method are easily available, and the price islow, the production cost can be greatly reduced while ensuring a high reaction yield, so that enlarged production is facilitated, meanwhile, the preparation method is different from the previous new preparation process, and the new preparation process is beneficial to academic research, industrial research and practice of ABTS in the field, so that the development of related technologies and related industrial economy in the field is promoted.

Method for synthesizing 2,2'-diamine-bis(3-ethylbenzothiazoline-6- sulfoacid)diamine salt

-

Paragraph 0018; 0020, (2018/11/22)

The invention provides a method for synthesizing 2,2'-diamine-bis(3-ethylbenzothiazoline-6-sulfoacid)diamine salt(ABTS), which belongs to the field of organic synthesis. According to the invention, 2-hydroxybenzothiazole is reacted with 2-ethyl bromide to form 3-ethylbenzothiazole-2-ketone, and then is reacted with hydrazine hydrate to generate 2,2'-azino-bis(3-ethylbenzothiazoline), 2,2'-azino-bis(3-ethylbenzothiazoline) is subjected to a sulfonation reaction with concentrated sulfuric acid to generate a compound 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfoacid), and finally the compound isreacted with ammonia gas to generate 2,2'-diamine-bis(3-ethylbenzothiazoline-6-sulfoacid)diamine salt. The raw materials used in the invention are cheap and easy to obtain, the operation is simple andconvenient, the reaction conditions are mild, and the yield is high.

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